EBIN DR. HAND PLUS SANITIZER

Manufacturer: WHAIN COSMETIC
Effective date: 2020-04-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:57

Label at a glance#

ProductEBIN DR. HAND PLUS SANITIZER

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EBIN

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73823-705-01	2023-01-30	C162847	48780-1	f386c64a-4150-0266-e053-dadaa90a7c1a	EBIN DR. HAND + SANITIZER 500 ml : 73823-705-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73823-705-01	EBIN DR. HAND PLUS SANITIZER	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73823-705	EBIN DR. HAND PLUS SANITIZER (ALCOHOL) GEL [WHAIN COSMETIC]	1	Legacy NDC, 1 package rows	20200430_a4783c5a-7473-478e-e053-2995a90a3c8d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

EBIN DR. HAND PLUS SANITIZER
ALCOHOL
AMINOMETHYL PROPANEDIOL
GLYCERIN
HYALURONATE SODIUM
BUTYLENE GLYCOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
ARTEMISIA PRINCEPS LEAF
GREEN TEA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73823-705	73823-705-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMINOMETHYL PROPANEDIOL	CZ7BU4QZJZ	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
ARTEMISIA PRINCEPS LEAF	SY077EW02G	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a4783bbd-6566-63f7-e053-2a95a90a2275			a4783c5a-7473-478e-e053-2995a90a3c8d	2020-04-29		Exact identifier spl id: a4783bbd-6566-63f7-e053-2a95a90a2275 spl set id: a4783c5a-7473-478e-e053-2995a90a3c8d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.